Benzyl­tributyl­ammonium 4,6-dihydroxy­naphthalene-2-sulfonate

The title mol­ecular salt, C(19)H(34)N(+)·C(10)H(7)O(5)S(−), is a charge-control agent used for toners in electrophotography with a high melting point of 508 K. In the crystal structure, the anions form inversion dimers, linked by pairs of O—H⋯O hydrogen bonds. Further O—H⋯O links between dimers gen...

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Detalles Bibliográficos
Autores principales: Uta, Kazuya, Mizuguchi, Jin
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968369/
https://www.ncbi.nlm.nih.gov/pubmed/21581927
http://dx.doi.org/10.1107/S1600536809000415
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author Uta, Kazuya
Mizuguchi, Jin
author_facet Uta, Kazuya
Mizuguchi, Jin
author_sort Uta, Kazuya
collection PubMed
description The title mol­ecular salt, C(19)H(34)N(+)·C(10)H(7)O(5)S(−), is a charge-control agent used for toners in electrophotography with a high melting point of 508 K. In the crystal structure, the anions form inversion dimers, linked by pairs of O—H⋯O hydrogen bonds. Further O—H⋯O links between dimers generate anionic sheets propagating in (010). One of the n-butyl chains of the cation is disordered over two sets of sites in a 0.53:0.47 ratio.
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spelling pubmed-29683692010-12-30 Benzyl­tributyl­ammonium 4,6-dihydroxy­naphthalene-2-sulfonate Uta, Kazuya Mizuguchi, Jin Acta Crystallogr Sect E Struct Rep Online Organic Papers The title mol­ecular salt, C(19)H(34)N(+)·C(10)H(7)O(5)S(−), is a charge-control agent used for toners in electrophotography with a high melting point of 508 K. In the crystal structure, the anions form inversion dimers, linked by pairs of O—H⋯O hydrogen bonds. Further O—H⋯O links between dimers generate anionic sheets propagating in (010). One of the n-butyl chains of the cation is disordered over two sets of sites in a 0.53:0.47 ratio. International Union of Crystallography 2009-01-17 /pmc/articles/PMC2968369/ /pubmed/21581927 http://dx.doi.org/10.1107/S1600536809000415 Text en © Uta and Mizuguchi 2009 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Uta, Kazuya
Mizuguchi, Jin
Benzyl­tributyl­ammonium 4,6-dihydroxy­naphthalene-2-sulfonate
title Benzyl­tributyl­ammonium 4,6-dihydroxy­naphthalene-2-sulfonate
title_full Benzyl­tributyl­ammonium 4,6-dihydroxy­naphthalene-2-sulfonate
title_fullStr Benzyl­tributyl­ammonium 4,6-dihydroxy­naphthalene-2-sulfonate
title_full_unstemmed Benzyl­tributyl­ammonium 4,6-dihydroxy­naphthalene-2-sulfonate
title_short Benzyl­tributyl­ammonium 4,6-dihydroxy­naphthalene-2-sulfonate
title_sort benzyl­tributyl­ammonium 4,6-dihydroxy­naphthalene-2-sulfonate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968369/
https://www.ncbi.nlm.nih.gov/pubmed/21581927
http://dx.doi.org/10.1107/S1600536809000415
work_keys_str_mv AT utakazuya benzyltributylammonium46dihydroxynaphthalene2sulfonate
AT mizuguchijin benzyltributylammonium46dihydroxynaphthalene2sulfonate

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